AMP-activated protein kinase

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Contents

Function

AMP-activated protein kinase (AMPK) is a nuclear receptor which regulates cellular uptake of glucose, β-oxidation of fatty acids and biogenesis of glucose transporter thus playing a role in cellular energy homeostasis by phosphorylating key proteins. In response to low levels of ATP, AMPK activates energy-producing pathways and inhibits energy-consuming pathways.

Relevance

AMPK is an important drug target for obesity, type 2 diabetes and cancer. AMPK activity is enhanced during exercise resulting in increased glucose uptake and blood supply in muscles. Stresses like hypoglycemia, anoxia and ischemia produce increase in AMPK levels.

Structural highlights

AMPK is a heterotrimer:
AMPK α subunit is the catalytic subunit and contains Thr174 (TPO) or Ser108 (SEP) which undergoes phosphorylation.
AMPK β subunit is a scaffold on which the heterotrimer assembles.
AMPK γ subunit detects shifts in AMP:ATP ratio via its 4 cystathionine β synthase (CBS) domains. The active site binds AMP.

3D structures of AMP-activated protein kinase

Updated on 01-November-2015

Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

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